Sr. Regulatory Affairs Manager
Katalyst HealthCares & Life Sciences
Job Description: The Senior Regulatory Affairs Manager will play a crucial role in leading and managing the regulatory submissions, including 510(k) and submissions. This individual will ensure compliance with all applicable regulations in the preparation of the submissions to FDA, provide regulatory guidance to cross-functional teams, and contribute to the successful approval and launch of innovative medical devices. Responsibilities: Prepare, review, and submit regulatory documents to FDA. Manage and oversee the regulatory submission process, ensuring timely and successful clearances/approvals. Ensure that all products comply with applicable regulatory requirements, including FDA regulations and ISO standards. Provide regulatory guidance to R&D team during product development life cycle. Stay updated on changes in regulatory requirements and communicate potential impacts to the organization. Conduct regulatory assessments for product changes and provide recommendations for appropriate regulatory pathways. Collaborate with internal stakeholders and external partners to ensure alignment on regulatory strategies and project timelines. Represent the company in meetings with regulatory agencies and external partners as needed. Ensure proper documentation and maintenance of regulatory submissions and correspondence with regulatory agencies. Requirements Master's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field; advanced degree preferred. Minimum of 7-10 years of experience in regulatory affairs within the medical device industry. Proven track record of leading and successfully obtaining 510(k) and clearances/approvals. Experience in interacting with FDA and other regulatory agencies. In-depth knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and other applicable medical device regulations. Strong leadership and project management skills, with the ability to manage multiple projects and priorities. Excellent communication, negotiation, and problem-solving skills. Ability to work collaboratively in a cross-functional team environment. Detail-oriented with strong organizational skills.
$154.4k - $231.6k
..., and impact.A Day in the LifeThis position sits within the Regulatory Affairs Data and Product Release group in the Medtronic Clinical & Regulatory... ...direction and people leadership, coaching and developing managers and teams to deliver timely, accurate, and compliant product...SeniorFull timeH1bWork at officeLocal areaImmediate startFlexible hours$154.4k - $231.6k
...impact. A Day in the Life This position sits within the Regulatory Affairs Data and Product Release group in the Medtronic Clinical &... ...strategic direction and people leadership, coaching and developing managers and teams to deliver timely, accurate, and compliant product...SeniorH1bWork at officeLocal areaImmediate startFlexible hours$154.4k - $231.6k
...A Day in the Life This position sits within the Regulatory Affairs Data and Product Release group in the Medtronic Clinical & Regulatory... ...strategic direction and people leadership, coaching and developing managers and teams to deliver timely, accurate, and compliant product...SeniorH1bWork at officeLocal areaFlexible hours$150k - $206.3k
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Principal Regulatory Affairs Project Manager - Medical Devices Global medical device manufacturer | Hybrid (3 days onsite) | Regulatory Affairs The role Our client, a long-established global leader in medical devices and combination products, is hiring a senior regulatory...$170k
Please see the below requirements for a Senior or Principal Electrical Engineer to join a growing class III medical device organization in the Northeast Twin Cities Metro. This role will play a critical part in supporting an implantable electromechanical system in a late...Senior$189k - $246k
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Senior Manager of Quality and Regulatory Plymouth, MN55441 Posted: 07/09/2026 Employment Type: Permanent Category: Business ProfessionalJob... ..., efficient, and risk-based execution of clinical affairs processes, as well as product verification and validation...SeniorPermanent employmentContract workLocal areaWorldwideFlexible hours$245k - $307.5k
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